Articles citing this paper
Sesquiterpenes From a New Zealand Sponge of the Genus Eurypon
CJ Barrow, JW Blunt and MHG Munro
41(11) pp.1755 - 1761
35 articles found in Crossref database.
13C-NMR of Natural Products (1992)
ChemInform Abstract: Sesquiterpenes from a New Zealand Sponge of the Genus Eurypon.
BARROW C. J.,
BLUNT J. W., MUNRO M. H. G.
ChemInform. 1989 20(27).
Marine natural products
Blunt John W.,
Copp Brent R.,
Hu Wan-Ping,
Munro Murray H. G.,
Northcote Peter T., Prinsep Michèle R.
Natural Product Reports. 2009 26(2). p.170
Short total synthesis of the spiro[4.5]decane sesquiterpene (−)-gleenol
Oesterreich Kai, Spitzner Dietrich
Tetrahedron. 2002 58(21). p.4331
Stereocontrolled Total Synthesis of (−)-Gleenol Using Claisen Rearrangement of Sterically Congested Dihydropyran
Nakazaki Atsuo,
Era Tomohiro, Kobayashi Susumu
Chemistry Letters. 2008 37(7). p.770
Uniquely Modified Imidazole Alkaloids from a Calcareous Leucetta Sponge
Edrada Ru Angelie,
Stessman Chad C., Crews Phillip
Journal of Natural Products. 2003 66(7). p.939
Dictionary of Terpenoids (1991)
Sesquiterpenes from the brown alga Taonia atomaria
De Rosa Salvatore,
De Giulio Alfonso,
Iodice Carmine, Zavodink Nevenka
Phytochemistry. 1994 37(5). p.1327
Antimalarial Isocyano and Isothiocyanato Sesquiterpenes with Tri- and Bicyclic Skeletons from the Nudibranch Phyllidia ocellata
White Andrew M.,
Pierens Gregory K.,
Skinner-Adams Tina,
Andrews Katherine T.,
Bernhardt Paul V.,
Krenske Elizabeth H.,
Mollo Ernesto, Garson Mary J.
Journal of Natural Products. 2015 78(6). p.1422
Dictionary of Organic Compounds (1990)
Tricyclic Sesquiterpenes from Marine Origin
Le Bideau Franck,
Kousara Mohammad,
Chen Li,
Wei Lai, Dumas Françoise
Chemical Reviews. 2017 117(9). p.6110
Micaryolanes A and B, Two New Caryolane‐Type Sesquiterpenoids from Marine Streptomyces sp. AH25
Wu Jiequn,
Zhu Yuqin,
Zhang Mengxue,
Li Hongji, Sun Peng
Chemistry & Biodiversity. 2020 17(12).
Recent advances on marine mollusk-derived natural products: chemistry, chemical ecology and therapeutical potential
Chen Zi-Hui,
Guo Yue-Wei, Li Xu-Wen
Natural Product Reports. 2023 40(3). p.509
The Anti‐Bredt Red Flag! Reassignment of Neoveratrenone
Savchenko Andrei I., Williams Craig M.
European Journal of Organic Chemistry. 2013 2013(32). p.7263
Facile Access to Spiro[4.5]decanes through Oxidative Dearomatization-Induced Ring Expansion of Cyclobutanes
Xi Shuang,
Zhang Jingyang,
Guo Zhen,
Zu Yumeng,
Liu Yang,
Wang Gelin, Tang Yefeng
Synthesis. 2022 54(18). p.3962
Do Anti‐Bredt Natural Products Exist? Olefin Strain Energy as a Predictor of Isolability
Krenske Elizabeth H., Williams Craig M.
Angewandte Chemie. 2015 127(36). p.10754
Do Anti‐Bredt Natural Products Exist? Olefin Strain Energy as a Predictor of Isolability
Krenske Elizabeth H., Williams Craig M.
Angewandte Chemie International Edition. 2015 54(36). p.10608
Encyclopedia of Marine Natural Products (2014)
Caryolene-forming carbocation rearrangements
Nguyen Quynh Nhu N, Tantillo Dean J
Beilstein Journal of Organic Chemistry. 2013 9 p.323
Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa
Wegerski Christopher J.,
Sonnenschein Rachel N.,
Cabriales Freddy,
Valeriote Frederick A.,
Matainaho Teatulohi, Crews Phillip
Tetrahedron. 2006 62(44). p.10393
Dictionary of Organic Compounds (1990)
Synthesis of (−)-Gleenol via C-H Insertion Reaction of Alkylidenecarbene
Ohira Susumu,
Yoshihara Naoya, Hasegawa Taisuke
Chemistry Letters. 1998 27(8). p.739
13C-NMR of Natural Products (1992)
Natural Products with Anti‐Bredt and Bridgehead Double Bonds
Mak Jeffrey Y. W.,
Pouwer Rebecca H., Williams Craig M.
Angewandte Chemie International Edition. 2014 53(50). p.13664
Encyclopedia of Marine Natural Products (2014)
Naturstoffe mit Anti‐Bredt‐ und Brückenkopf‐Doppelbindung
Mak Jeffrey Y. W.,
Pouwer Rebecca H., Williams Craig M.
Angewandte Chemie. 2014 126(50). p.13882
New Sesquiterpene Ethers from Vetiver Oil
Weyerstahl Peter,
Marschall Helga,
Splittgerber Ute, Wolf Dietmar
Liebigs Annalen. 1996 1996(7). p.1195
Silicon guided rearrangement of epoxydecalines to spirocyclic compounds. Synthesis of gleenol and axenol from carvone
Blay Gonzalo,
Collado Ana M.,
García Begoña, Pedro José R.
Tetrahedron. 2005 61(46). p.10853
Total Synthesis of (.+-.)-Gleenol and (.+-.)-Axenol via a Functionalized Spiro[4.5]decane
Nakazaki Atsuo,
Era Tomohiro, Kobayashi Susumu
Chemical and Pharmaceutical Bulletin. 2007 55(11). p.1606
Synthesis of Sesquiterpenes via Silicon-Guided Rearrangement of Epoxydecalins
Blay Gonzalo,
Collado Ana M.,
García Begoña, Pedro José R.
Natural Product Communications. 2008 3(3). p.1934578X0800300
Stereoselective total synthesis of (±)-α-vetispirene, (±)-hinesol, and (±)-β-vetivone based on a Claisen rearrangement
Nakazaki Atsuo,
Era Tomohiro,
Numada Yuko, Kobayashi Susumu
Tetrahedron. 2006 62(26). p.6264
Minor components in the essential oil of Juniperus oxycedrus L. wood
Barrero Alejandro F.,
Oltra J. Enrique,
Altarejos Joaquíin,
Barragán Armando,
Lara Armando, Laurent Raymond
Flavour and Fragrance Journal. 1993 8(4). p.185
A unified, RCM anchored approach to spiro[4.5]decane-based sesquiterpenoids: Collective synthesis of (±)-α & β-vetispirenes, (±)-β-vetivone, (±)-agarospirol and (±)-hinesol
Athe Sudhakar,
Ghosh Subhash, Mehta Goverdhan
Tetrahedron Letters. 2019 60(24). p.1570
Organic Synthesis: Theory and Applications Volume 5 (2001)
A New Tricyclo[6.3.1.02,5]dodecane Sesquiterpene from Cultures of the Basidiomycete Campanella junghuhnii
Liu Rong,
Zhou Zhong‐Yu,
Xu Di,
Wang Fei, Liu Ji‐Kai
Helvetica Chimica Acta. 2009 92(2). p.375
